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Journal of Human Genetics|April 23, 2011
Dysbindin-1 and NRG-1 gene expression in immortalized lymphocytes from patients with schizophreniaHidenaga Yamamori, Ryota Hashimoto, Louise Verrall, et al.Journal of Human Genetics|July 22, 2011
Association of a synonymous GAT3 polymorphism with antiepileptic drug pharmacoresistanceDong-Uk Kim, Myeong-Kyu Kim, Yong-Won Cho, et al.Journal of Human Genetics|July 29, 2011
Screening of genetic variations of SLC15A2, SLC22A1, SLC22A2 and SLC22A6 genesHyun Sub Cheong, Hae Deun Kim, Han Sung Na, et al.Journal of Human Genetics|July 15, 2011
Genetic analysis of contiguous X-chromosome deletion syndrome encompassing the BTK and TIMM8A genesTakashi Arai, Meina Zhao, Hirokazu Kanegane, et al.Journal of Human Genetics|July 15, 2011
Genetic features of ancient West Siberian people of the Middle Ages, revealed by mitochondrial DNA haplogroup analysisTakehiro Sato, Dmitry Razhev, Tetsuya Amano, et al.Journal of Human Genetics|August 19, 2011
Remapping and mutation analysis of benign adult familial myoclonic epilepsy in a Japanese pedigreeSatsuki Mori, Masayuki Nakamura, Takeshi Yasuda, et al.Journal of Human Genetics|August 19, 2011
Mutations in mitochondrially encoded complex I enzyme as the second common cause in a cohort of Chinese patients with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodesDanhua Zhao, Daojun Hong, Wei Zhang, et al.Journal of Human Genetics|August 12, 2011
Mitochondrial DNA and Y-chromosome microstructure in TunisiaHajer Ennafaa, Rosa Fregel, Houssein Khodjet-El-Khil, et al.Journal of Human Genetics|September 9, 2011
Genome-wide association study identifies genetic variants in GOT1 determining serum aspartate aminotransferase levelsHaiqing Shen, Coleen Damcott, Scott R Shuldiner, et al.Journal of Human Genetics|September 9, 2011
Identification of independent risk loci for Graves' disease within the MHC in the Japanese populationKazuhiko Nakabayashi, Atsushi Tajima, Ken Yamamoto, et al.Pageof 351